Tricaud Nicolas, Gautier Benoit, Berthelot Jade, Gonzalez Sergio, Van Hameren Gerben
Institut des Neurosciences de Montpellier, Univ. Montpellier, INSERM, 34000 Montpellier, France.
I-Stem, UEVE/UPS U861, INSERM U861, AFM, 91100 Corbeil-Essonnes, France.
Biomedicines. 2022 Jun 19;10(6):1447. doi: 10.3390/biomedicines10061447.
A large number of peripheral neuropathies, among which are traumatic and diabetic peripheral neuropathies, result from the degeneration of the myelin sheath, a process called demyelination. Demyelination does not result from Schwann cell death but from Schwann cell dedifferentiation, which includes reprograming and several catabolic and anabolic events. Starting around 4 h after nerve injury, activation of MAPK/cJun pathways is the earliest characterized step of this dedifferentiation program. Here we show, using real-time in vivo imaging, that Schwann cell mitochondrial pH, motility and calcium content are altered as soon as one hour after nerve injury. Mitochondrial calcium release occurred through the VDAC outer membrane channel and mPTP inner membrane channel. This calcium influx in the cytoplasm induced Schwann-cell demyelination via MAPK/c-Jun activation. Blocking calcium release through VDAC silencing or VDAC inhibitor TRO19622 prevented demyelination. We found that the kinetics of mitochondrial calcium release upon nerve injury were altered in the Schwann cells of diabetic mice suggesting a permanent leak of mitochondrial calcium in the cytoplasm. TRO19622 treatment alleviated peripheral nerve defects and motor deficit in diabetic mice. Together, these data indicate that mitochondrial calcium homeostasis is instrumental in the Schwann cell demyelination program and that blocking VDAC constitutes a molecular basis for developing anti-demyelinating drugs for diabetic peripheral neuropathy.
大量的周围神经病变,其中包括创伤性和糖尿病性周围神经病变,是由髓鞘变性引起的,这一过程称为脱髓鞘。脱髓鞘并非由施万细胞死亡导致,而是由施万细胞去分化引起的,这包括重新编程以及一些分解代谢和合成代谢事件。从神经损伤后约4小时开始,MAPK/cJun通路的激活是该去分化程序最早被表征的步骤。在这里,我们使用实时体内成像显示,神经损伤后一小时,施万细胞的线粒体pH值、运动性和钙含量就会发生改变。线粒体钙释放通过VDAC外膜通道和mPTP内膜通道发生。这种钙流入细胞质通过MAPK/c-Jun激活诱导施万细胞脱髓鞘。通过VDAC沉默或VDAC抑制剂TRO19622阻断钙释放可防止脱髓鞘。我们发现,糖尿病小鼠施万细胞中神经损伤后线粒体钙释放的动力学发生了改变,这表明线粒体钙在细胞质中存在永久性泄漏。TRO19622治疗减轻了糖尿病小鼠的周围神经缺陷和运动功能障碍。总之,这些数据表明线粒体钙稳态在施万细胞脱髓鞘程序中起作用,并且阻断VDAC构成了开发用于治疗糖尿病性周围神经病变的抗脱髓鞘药物的分子基础。